NUP214 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5114371-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5114371 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
NUP214
Classification
Polyclonal
Conjugate
Unconjugated
Gene
NUP214
Gene Alias
214 kDa nucleoporin; BC039282; CAIN; CAN; CAN protein, putative oncogene; D2H9S46E; Kiaa0023; Nuclear pore complex protein Nup214; nucleoporin 214; nucleoporin 214kDa; nucleoporin Nup214; Nup214; Protein CAN; RGD1304977
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
8021
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Lyophilized
Applications
ELISA, Flow Cytometry, Immunocytochemistry, Western Blot
Concentration
500 μg/mL
Formulation
PBS with 4MG trehalose and 0.05MG sodium azide
Gene Accession No.
P35658
Gene Symbols
NUP214
Immunogen
E.coli-derived human NUP214 recombinant protein (Position: K36-E374).
Quantity
100 μg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 μg/mL
- The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm
- Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells
- This gene is a member of the FG-repeat-containing nucleoporins
- The protein encoded by this gene is localized to the cytoplasmic face of the nuclear pore complex where it is required for proper cell cycle progression and nucleocytoplasmic transport
- The 3' portion of this gene forms a fusion gene with the DEK gene on chromosome 6 in a t(6,9) translocation associated with acute myeloid leukemia and myelodysplastic syndrome
- Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.